Patent classifications
A61K31/436
Treatment of asthma and chronic obstructive pulmonary disease with anti-proliferate and anti-inflammatory drugs
Embodiments of the present invention provide a method for treatment of respiratory disorders such as asthma, chronic obstructive pulmonary disease, and chronic sinusitis, including cystic fibrosis, interstitial fibrosis, chronic bronchitis, emphysema, bronchopulmonary dysplasia and neoplasia. The method involves administration, preferably oral, nasal or pulmonary administration, of anti-inflammatory and anti-proliferative drugs (rapamycin or paclitaxel and their analogues) and an additive.
Compositions and methods for treating cancer
Disclosed are methods for treating cancer by reduction of glycogen stores and administering tyrosine derivatives.
Compositions and methods for treating cancer
Disclosed are methods for treating cancer by reduction of glycogen stores and administering tyrosine derivatives.
Compositions and methods for treating cancer
Disclosed are methods for treating cancer by reduction of glycogen stores and administering tyrosine derivatives.
VETERINARY FORMULATIONS COMPRISING RAPAMYCIN AND METHODS OF USING THE SAME FOR TREATING ANIMAL DISEASE
The present disclosure provides veterinary formulations comprising rapamycin or rapalogs for administration to companion animals and methods of using the formulations to treat cardiac dysfunction, including hypertrophic cardiomyopathy, dilated cardiomyopathy, mitral valve disease, pressure-overload cardiac hypertrophy, cancer, effects of aging, inflammatory disease, and viral infection.
VETERINARY FORMULATIONS COMPRISING RAPAMYCIN AND METHODS OF USING THE SAME FOR TREATING ANIMAL DISEASE
The present disclosure provides veterinary formulations comprising rapamycin or rapalogs for administration to companion animals and methods of using the formulations to treat cardiac dysfunction, including hypertrophic cardiomyopathy, dilated cardiomyopathy, mitral valve disease, pressure-overload cardiac hypertrophy, cancer, effects of aging, inflammatory disease, and viral infection.
COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF HIF2-alpha AND THEIR METHODS OF USE
- Robin Alec FAIRHURST ,
- Christine FRITSCH ,
- Marc Gerspacher ,
- Jürgen Hans-Hermann HINRICHS ,
- Jean-Baptiste Georges Armand LANGLOIS ,
- Catherine Leblanc ,
- Tengfei LI ,
- Edwige Liliane Jeanne Lorthiois ,
- Christophe Mura ,
- Cristina Montserrat NIETO-OBERHUBER ,
- Milen TODOROV ,
- Andrea Vaupel ,
- Nicolas WARIN ,
- Rainer Wilcken
The present invention relates to compounds of formula (I)
##STR00001##
or a pharmaceutically acceptable salt form thereof, wherein the substituents are as defined in the specification; to intermediates in the preparation of the compounds, to pharmaceutical compositions comprising the compounds and to the use of the compounds in the treatment of disease.
COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF HIF2-alpha AND THEIR METHODS OF USE
- Robin Alec FAIRHURST ,
- Christine FRITSCH ,
- Marc Gerspacher ,
- Jürgen Hans-Hermann HINRICHS ,
- Jean-Baptiste Georges Armand LANGLOIS ,
- Catherine Leblanc ,
- Tengfei LI ,
- Edwige Liliane Jeanne Lorthiois ,
- Christophe Mura ,
- Cristina Montserrat NIETO-OBERHUBER ,
- Milen TODOROV ,
- Andrea Vaupel ,
- Nicolas WARIN ,
- Rainer Wilcken
The present invention relates to compounds of formula (I)
##STR00001##
or a pharmaceutically acceptable salt form thereof, wherein the substituents are as defined in the specification; to intermediates in the preparation of the compounds, to pharmaceutical compositions comprising the compounds and to the use of the compounds in the treatment of disease.
Imidazo[4,5-C]pyridine derived SSAO inhibitors
A compound of formula (I) or a pharmaceutically acceptable salt, or N-oxide thereof and the use of the same in therapy: wherein Z, Y, R.sup.1, W, V, and R.sup.3 are as defined in claim 1. ##STR00001##
Imidazo[4,5-C]pyridine derived SSAO inhibitors
A compound of formula (I) or a pharmaceutically acceptable salt, or N-oxide thereof and the use of the same in therapy: wherein Z, Y, R.sup.1, W, V, and R.sup.3 are as defined in claim 1. ##STR00001##